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Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost
Bradykinesia is the most disabling motor symptom of Parkinson’s disease (PD). The sequence effect (SE), a feature of bradykinesia, refers to the rapid decrement in amplitude and speed of repetitive movements (e.g., gait, handwriting) and is a major cause of morbidity in PD. Previous research has rev...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877367/ https://www.ncbi.nlm.nih.gov/pubmed/27252678 http://dx.doi.org/10.3389/fneur.2016.00083 |
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author | Tinaz, Sule Pillai, Ajay S. Hallett, Mark |
author_facet | Tinaz, Sule Pillai, Ajay S. Hallett, Mark |
author_sort | Tinaz, Sule |
collection | PubMed |
description | Bradykinesia is the most disabling motor symptom of Parkinson’s disease (PD). The sequence effect (SE), a feature of bradykinesia, refers to the rapid decrement in amplitude and speed of repetitive movements (e.g., gait, handwriting) and is a major cause of morbidity in PD. Previous research has revealed mixed results regarding the role of dopaminergic treatment in the SE. However, external cueing has been shown to improve it. In this study, we aimed to characterize the SE systematically and relate this phenomenon to the energetic cost of movement within the context of cost–benefit framework of motor control. We used a dynamic isometric motor task with auditory pacing to assess the SE in motor output during a 15-s task segment in PD patients and matched controls. All participants performed the task with both hands, and without and with visual feedback (VF). Patients were also tested in “on”- and “off”-dopaminergic states. Patients in the “off” state did not show higher SE compared to controls, partly due to large variance in their performance. However, patients in the “on” state and in the absence of VF showed significantly higher SE compared to controls. Patients expended higher total motor energy compared to controls in all conditions and regardless of their medication status. In this experimental situation, the SE in PD is associated with the cumulative energetic cost of movement. Dopaminergic treatment, critical for internal triggering of movement, fails to maintain the motor vigor across responses. The high motor cost may be related to failure to incorporate limbic/motivational cues into the motor plan. VF may facilitate performance by shifting the driving of movement from internal to external or, alternatively, by functioning as a motivational cue. |
format | Online Article Text |
id | pubmed-4877367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48773672016-06-01 Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost Tinaz, Sule Pillai, Ajay S. Hallett, Mark Front Neurol Neuroscience Bradykinesia is the most disabling motor symptom of Parkinson’s disease (PD). The sequence effect (SE), a feature of bradykinesia, refers to the rapid decrement in amplitude and speed of repetitive movements (e.g., gait, handwriting) and is a major cause of morbidity in PD. Previous research has revealed mixed results regarding the role of dopaminergic treatment in the SE. However, external cueing has been shown to improve it. In this study, we aimed to characterize the SE systematically and relate this phenomenon to the energetic cost of movement within the context of cost–benefit framework of motor control. We used a dynamic isometric motor task with auditory pacing to assess the SE in motor output during a 15-s task segment in PD patients and matched controls. All participants performed the task with both hands, and without and with visual feedback (VF). Patients were also tested in “on”- and “off”-dopaminergic states. Patients in the “off” state did not show higher SE compared to controls, partly due to large variance in their performance. However, patients in the “on” state and in the absence of VF showed significantly higher SE compared to controls. Patients expended higher total motor energy compared to controls in all conditions and regardless of their medication status. In this experimental situation, the SE in PD is associated with the cumulative energetic cost of movement. Dopaminergic treatment, critical for internal triggering of movement, fails to maintain the motor vigor across responses. The high motor cost may be related to failure to incorporate limbic/motivational cues into the motor plan. VF may facilitate performance by shifting the driving of movement from internal to external or, alternatively, by functioning as a motivational cue. Frontiers Media S.A. 2016-05-24 /pmc/articles/PMC4877367/ /pubmed/27252678 http://dx.doi.org/10.3389/fneur.2016.00083 Text en Copyright © 2016 Tinaz, Pillai and Hallett. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Tinaz, Sule Pillai, Ajay S. Hallett, Mark Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost |
title | Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost |
title_full | Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost |
title_fullStr | Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost |
title_full_unstemmed | Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost |
title_short | Sequence Effect in Parkinson’s Disease Is Related to Motor Energetic Cost |
title_sort | sequence effect in parkinson’s disease is related to motor energetic cost |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877367/ https://www.ncbi.nlm.nih.gov/pubmed/27252678 http://dx.doi.org/10.3389/fneur.2016.00083 |
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